DocuSign Automated Testing Accelerated

Get automated testing, validation lifecycle management, and application lifecycle management in a single app.

DocuSign helps life sciences organizations automate the preparation, signing, and management of agreements. It enables U.S. Food and Drug Administration (FDA) 21 CFR Part 11 and Health Insurance Portability and Accountability Act (HIPAA) compliant eSignatures. It’s the world’s first choice for electronic signatures on practically any device.

ProcessX and DocuSign

By automating testing, Validation Lifecycle Management (VLM), and Application Lifecycle Management (ALM) in ProcessX, you’re able to:

  • Integrate VLM and change control to eliminate process deviations
  • Access real-time dashboards to see the status of a release and compliance activities
  • Achieve faster test execution to free your team of burdensome validation tasks
  • Enable workflow-enforced Quality by Design
  • Streamline collaboration between IT, quality, and business teams
  • Experience fewer data-entry errors by digitalizing and automating paper-based workflows
  • Improve quality with regulatory requirements management using AI

Automated Testing and Validation Workflows

Regulatory Artifacts and On-Demand Reporting

ProcessX delivers out-of-the-box reporting templates and dashboards that save you time and give you peace of mind that you are audit-ready at a moment’s notice. Regulatory artifacts and reports include:

  • Validation plan
  • Requirements (with detailed risk assessment applied)
  • Risk-based automation and configuration verification tests (IQ, OQ, and PQ)
  • Traceability reports (generated in real-time to maintain full visibility digitally or via extracted matrices)
  • Validation and verification protocols for initial validation and subsequent release management (the reports contain all mitigation evidence, risk assessments, traceability, and rationales for the release)

 

The DocuSign and USDM partnership has resulted in deployments at the Top 20 global biopharma and medical device companies and in high-growth life sciences organizations.

USDM has perfected DocuSign implementation to get you up and running in as fast as seven days. There’s no need to create your documents from scratch; we’ve optimized more than 175 DocuSign systems using our methodologies, document templates, and processes. From there, system configurations can be modified using change control processes.

Streamline and optimize your GxP workflows and DocuSign electronic signatures with ProcessX and reduce your compliance costs by up to 80%!

Get in touch with our team to optimize your GxP processes today!